About The Medical Condition Deficiency Disease, Galactokinase
Find the definition of the medical term Deficiency Disease, Galactokinase. Deficiency Disease, Galactokinase defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Deficiency Disease, Galactokinase
| Deficiency Disease, Galactokinase Medical Condition |
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What's The Definition Of The Medical Condition Deficiency Disease, Galactokinase?
A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (OVARIAN FAILURE, PREMATURE); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)
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